Canonical Allele Identifier: CA1130406594
Gene: CSF2RA HGNC NCBI

Linked Data

dbSNP Id: rs2091274949

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.1290261_1290282del , CM000685.2:g.1290261_1290282del GRCh38
NC_000023.10:g.1409154_1409175del , CM000685.1:g.1409154_1409175del GRCh37
NC_000023.9:g.1369154_1369175del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000498153.7:c.474-76_474-55del ENSP00000512483.1:n.474-76_474-55del
ENST00000696230.1:c.*557-76_*557-55del ENSP00000512496.1:n.*557-76_*557-55del
ENST00000381529.9:c.474-76_474-55del MANE Select ENSP00000370940.3:n.474-76_474-55del
ENST00000432318.8:c.474-76_474-55del ENSP00000416437.2:n.474-76_474-55del
ENST00000355432.8:c.474-76_474-55del ENSP00000347606.3:n.474-76_474-55del
ENST00000355805.7:c.474-76_474-55del ENSP00000348058.2:n.474-76_474-55del
ENST00000381500.6:c.474-76_474-55del ENSP00000370911.1:n.474-76_474-55del
ENST00000381509.8:c.474-76_474-55del ENSP00000370920.3:n.474-76_474-55del
ENST00000381524.8:c.474-76_474-55del ENSP00000370935.3:n.474-76_474-55del
ENST00000381529.8:c.474-76_474-55del ENSP00000370940.3:n.474-76_474-55del
ENST00000412290.6:c.474-76_474-55del ENSP00000410667.1:n.474-76_474-55del
ENST00000417535.7:c.474-76_474-55del ENSP00000394227.2:n.474-76_474-55del
ENST00000419094.6:c.474-76_474-55del ENSP00000397452.1:n.474-76_474-55del
ENST00000432318.7:c.474-76_474-55del ENSP00000416437.2:n.474-76_474-55del
ENST00000486791.6:c.474-76_474-55del ENSP00000436825.1:n.474-76_474-55del
ENST00000493312.6:n.511-76_511-55del
ENST00000494969.7:c.244+3063_244+3084del ENSP00000476684.1:n.244+3063_244+3084del
ENST00000501036.7:c.75-76_75-55del ENSP00000440491.1:n.75-76_75-55del
XM_011546165.1:c.474-76_474-55del XP_011544467.1:n.474-76_474-55del
XM_011546166.1:c.474-76_474-55del XP_011544468.1:n.474-76_474-55del
XM_011546167.1:c.474-76_474-55del XP_011544469.1:n.474-76_474-55del
XM_011546168.1:c.474-76_474-55del XP_011544470.1:n.474-76_474-55del
XM_011546169.1:c.474-76_474-55del XP_011544471.1:n.474-76_474-55del
XM_011546170.1:c.474-76_474-55del XP_011544472.1:n.474-76_474-55del
XM_011546171.1:c.474-76_474-55del XP_011544473.1:n.474-76_474-55del
XM_011546172.1:c.474-76_474-55del XP_011544474.1:n.474-76_474-55del
XM_011546173.1:c.474-76_474-55del XP_011544475.1:n.474-76_474-55del
XM_011546174.1:c.474-76_474-55del XP_011544476.1:n.474-76_474-55del
XM_011546175.1:c.474-76_474-55del XP_011544477.1:n.474-76_474-55del
XM_011546176.1:c.342-76_342-55del XP_011544478.1:n.342-76_342-55del
XM_011546165.3:c.474-76_474-55del XP_011544467.1:n.474-76_474-55del
XM_011546167.2:c.474-76_474-55del XP_011544469.1:n.474-76_474-55del
XM_011546168.2:c.474-76_474-55del XP_011544470.1:n.474-76_474-55del
XM_011546170.3:c.474-76_474-55del XP_011544472.1:n.474-76_474-55del
XM_011546174.3:c.474-76_474-55del XP_011544476.1:n.474-76_474-55del
XM_011546175.2:c.474-76_474-55del XP_011544477.1:n.474-76_474-55del
XM_017029287.1:c.474-76_474-55del XP_016884776.1:n.474-76_474-55del
XM_017029288.1:c.474-76_474-55del XP_016884777.1:n.474-76_474-55del